Copertina di Erondu–Cymet Syndrome
Titolo del libro:

Erondu–Cymet Syndrome

Chromosome 21 (human), Karyotype, Tyler Cymet, Down syndrome, Human Genome Project

Cede Publishing (06.03.2012 )

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ISBN-13:

978-620-0-83887-2

ISBN-10:
6200838879
EAN:
9786200838872
Lingua del libro:
Inglese
Risvolto di copertina:
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Erondu–Cymet syndrome is a syndrome caused by a translocation on the . The genetic for people with this condition is 46, XY, inv(21)(q11.2q22.1). Findings in these patients include: hypotension, hypoxemia, seizures, and impairment of cognitive ability. Patients with this condition may have persistent left superior vena cava that drains into the left atrium, as well as pulmonary arterio-venous malformations. Erondu–Cymet Syndrome was discovered in 2006 by Ugochi Erondu and . In 2000, researchers working on the announced that they had determined the sequence of that make up this chromosome. Chromosome 21 was the second human chromosome to be fully sequenced.
Casa editrice:
Cede Publishing
Sito Web:
http://www.alphascript-publishing.com
A cura di:
Barnabas Cristóbal
Numero di pagine:
52
Pubblicato il:
06.03.2012
Giacenza di magazzino:
Disponibile
categoria:
Biologia
Prezzo:
1.026,89 NT$
Parole chiave:
karyotype, Down syndrome, Human Genome Project, Chromosome 21 (human), Tyler Cymet

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